|
ENST00000269217.11:c.3516T=
MANE Plus Clinical
|
ENSP00000269217.5:p.Thr1172=
|
|
|
ENST00000313654.14:c.8343T=
MANE Select
|
ENSP00000324532.8:p.Thr2781=
|
|
|
ENST00000649721.1:c.4938T=
|
ENSP00000497885.1:p.Thr1646=
|
|
|
ENST00000269217.10:c.3516T=
|
ENSP00000269217.5:p.Thr1172=
|
|
|
ENST00000313654.13:c.8343T=
|
ENSP00000324532.8:p.Thr2781=
|
|
|
ENST00000399516.7:c.8175T=
|
ENSP00000382432.2:p.Thr2725=
|
|
|
ENST00000586751.5:c.3121T=
|
|
|
|
ENST00000587184.5:c.3348T=
|
ENSP00000466557.1:p.Thr1116=
|
|
|
ENST00000588164.2:c.48T=
|
ENSP00000467473.2:p.Thr16=
|
|
|
ENST00000588770.5:n.2921T=
|
|
|
|
NM_000227.4:c.3516T=
|
NP_000218.3:p.Thr1172=
|
|
|
NM_001127717.2:c.8175T=
|
NP_001121189.2:p.Thr2725=
|
|
|
NM_001127718.2:c.3348T=
|
NP_001121190.2:p.Thr1116=
|
|
|
NM_198129.2:c.8343T=
|
NP_937762.2:p.Thr2781=
|
|
|
XM_011525978.1:c.8370T=
|
XP_011524280.1:p.Thr2790=
|
|
|
XM_011525979.1:c.8361T=
|
XP_011524281.1:p.Thr2787=
|
|
|
XM_011525980.1:c.8352T=
|
XP_011524282.1:p.Thr2784=
|
|
|
XM_011525981.1:c.8238T=
|
XP_011524283.1:p.Thr2746=
|
|
|
XM_011525982.1:c.8073T=
|
XP_011524284.1:p.Thr2691=
|
|
|
XM_011525978.2:c.8370T=
|
XP_011524280.1:p.Thr2790=
|
|
|
XM_011525979.2:c.8361T=
|
XP_011524281.1:p.Thr2787=
|
|
|
XM_011525980.2:c.8352T=
|
XP_011524282.1:p.Thr2784=
|
|
|
XM_011525981.2:c.8238T=
|
XP_011524283.1:p.Thr2746=
|
|
|
XM_011525982.2:c.8073T=
|
XP_011524284.1:p.Thr2691=
|
|
|
XM_017025743.1:c.6222T=
|
XP_016881232.1:p.Thr2074=
|
|
|
XM_017025744.1:c.3912T=
|
XP_016881233.1:p.Thr1304=
|
|
|
XR_001753199.1:n.8611T=
|
|
|
|
NM_000227.5:c.3516T=
|
NP_000218.3:p.Thr1172=
|
|
|
NM_001127717.3:c.8175T=
|
NP_001121189.2:p.Thr2725=
|
|
|
NM_001127718.3:c.3348T=
|
NP_001121190.2:p.Thr1116=
|
|
|
NM_198129.3:c.8343T=
|
NP_937762.2:p.Thr2781=
|
|
|
NM_000227.6:c.3516T=
MANE Plus Clinical
|
NP_000218.3:p.Thr1172=
|
|
|
NM_001127717.4:c.8175T=
|
NP_001121189.2:p.Thr2725=
|
|
|
NM_001127718.4:c.3348T=
|
NP_001121190.2:p.Thr1116=
|
|
|
NM_198129.4:c.8343T=
MANE Select
|
NP_937762.2:p.Thr2781=
|
|
